AFF1基因标记为橘红色,总长度为715kb; KMT2A基因标记为绿色,长度为982kb。 临床意义 急性淋巴细胞白血病ALL 急性粒细胞白血病AML 辅助诊断KMT2A::AFF1融合的急性白血病。人KMT2A/MLL基因的染色体重排与新发及治疗诱导的婴儿、儿童和成人急性白血病相关。研究显示,KMT2A的伙伴基因多达100多种,七种最常见的TPG和PT...
KMT2A-AFF1 TranslocationEnquiry Product Description Product database CBP20193D FormatDNA Description KMT2A (Lysine Methyltransferase 2A) is a Protein Coding gene. Diseases associated with KMT2A include Wiedemann-Steiner Syndrome and Acute Myeloid Leukemia With T(9;11)(P22;Q23). Among its related pa...
KMT2A/AFF1融合基因检测-分子病理-广州安必平医药科技股份有限公司(股票代码:688393)专注于肿瘤筛查与诊断,自主研发了一系列肿瘤筛查及诊断试剂与配套设备,主要应用科室为病理科。目前已搭建液基细胞学(LBP)、聚合酶链式反应(PCR)、免疫组织化学(IHC)和荧光原位
脾脏及骨髓的HE染色和CD45 /B220þ白血病细胞计数发现Amlexanox抑制了KMT2A / AFF1小鼠模型中前B细胞白血病的浸润。 4.在KMT2A / AFF1 Tg小鼠体内Amlexanox通过p53–caspase-3凋亡途径抑制S100A6上调 为了研究Amlexanox在KMT2A / AF...
名称KMT2A-AFF1 Translocation 型号CBP20193D 报价 特点KMT2A-AFF1 Translocation 详细内容 CBP20193D FormatDNA Description KMT2A (Lysine Methyltransferase 2A) is a Protein Coding gene. Diseases associated with KMT2A include Wiedemann-Steiner Syndrome and Acute Myeloid Leukemia With T(9;11)(P22;Q23)....
名称KMT2A(E8)-AFF1(E6) Fusion 型号CBP20193R 报价 特点KMT2A(E8)-AFF1(E6) Fusion 详细内容 Introduction FormatRNA DescriptionN/A Technical Data Left GeneKMT2A Left Breakpointchr11:118353210:+ Right GeneAFF1 Right Breakpointchr4:88011136:+ ...
摘要 目的分析伴KMT2A::AFF1基因阳性急性B淋巴细胞白血病(B-ALL)的临床特点与患者预后及其预后风险因素的相关性。方法回顾性队列研究。纳入2011年4月1日至2022年7月31日上海市第一人民医院和海军军医大学附属...展开更多 Objective To analyze the correlation between clinical features and prognosis or prognostic ...
Prognostic impact of KMT2A‐AFF1‐positivity in 926 BCR‐ABL1‐negative B‐lineage acute lymphoblastic leukemia patients treated in GIMEMA clinical trials since 1996doi:10.1002/ajh.26253Alfonso PiciocchiMonica MessinaLoredana EliaAntonella Vitale
Hindawi Case Reports in Hematology Volume 2019, Article ID 7394619, 4 pages https://doi.org/10.1155/2019/7394619 Case Report Immunotherapy- (Blinatumomab-) Related Lineage Switch of KMT2A/AFF1 Rearranged B-Lymphoblastic Leukemia into Acute Myeloid Leukemia/Myeloid Sarcoma and Subsequently into B/...
在急性白血病治疗过程中系别转化罕见,在与系别转化相关的染色体畸变中,t(4;11)(q21;q23)与KMT2A/AFF1 融合蛋白[原混合谱系白血病(mixed linage leukemia,MLL)基因 MLL/AFF1 或 MLL/AF4 ]重排最为常见[1 ].研究表明,MLL重排...